메뉴 건너뛰기




Volumn 12, Issue 16, 2010, Pages 3686-3689

β-selective arabinofuranosylation using a 2,3-o-xylylene-protected donor

Author keywords

[No Author keywords available]

Indexed keywords

DRUG DERIVATIVE; LIPOARABINOMANNAN; LIPOPOLYSACCHARIDE; MANNOSE; OLIGOSACCHARIDE; XYLENE;

EID: 77955679176     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101520q     Document Type: Article
Times cited : (60)

References (49)
  • 1
    • 0004106191 scopus 로고    scopus 로고
    • 2nd ed.; Varki, A., Cummings, R. D., Esko, J. D., Freeze, H. H., Stanley, P., Bertozzi, C. R., Hart, G. W., Etzler, M. E., Eds.; Cold Spring Harbor Laboratory Press: New York
    • Essentials of Glycobiology, 2nd ed.; Varki, A., Cummings, R. D., Esko, J. D., Freeze, H. H., Stanley, P., Bertozzi, C. R., Hart, G. W., Etzler, M. E., Eds.; Cold Spring Harbor Laboratory Press: New York, 2009.
    • (2009) Essentials of Glycobiology
  • 4
    • 0004288915 scopus 로고    scopus 로고
    • Hanessian, S., Ed.; Marcel Dekker, Inc.: New York
    • Preparative Carbohydrate Chemistry; Hanessian, S., Ed.; Marcel Dekker, Inc.: New York, 1997.
    • (1997) Preparative Carbohydrate Chemistry
  • 10
    • 77955688262 scopus 로고    scopus 로고
    • For reviews, see
    • For reviews, see
  • 30
    • 77955671777 scopus 로고    scopus 로고
    • Biasing the conformation of a pyranose ring with a cis-butenyl linker has been reported, but the use of this species in glycosylation reactions has not
    • Biasing the conformation of a pyranose ring with a cis-butenyl linker has been reported, but the use of this species in glycosylation reactions has not.
  • 32
    • 77955699092 scopus 로고    scopus 로고
    • note
    • It should be noted that a glycosylation with a 2,3-di-O-tetra-i- propyldisiloxane-protected arabinofuranose thioglycoside has been reported (ref 11d); the α/β selectivity was 1:2.5.
  • 34
    • 77955672577 scopus 로고    scopus 로고
    • The purification of the product after the introduction of the xylylene group was difficult. However, removal of the TBDPS group made it easier to separate 5 from other reaction byproducts
    • The purification of the product after the introduction of the xylylene group was difficult. However, removal of the TBDPS group made it easier to separate 5 from other reaction byproducts.
  • 42
    • 77955699304 scopus 로고    scopus 로고
    • Unpublished investigations
    • Joe, M.; Lowary, T. L. Unpublished investigations.
    • Joe, M.1    Lowary, T.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.